Evidence map›Paper›PMID 40360583›Full record

ArticleScientific reports2025

Serum glial fibrillary protein reflects early brain injury dynamics and cognitive changes after deep brain stimulation surgery.

Anika Frank, Jonas Arjomand, Jonas Bendig, Mia Delfs, Lisa Klingelhoefer, Witold H Polanski, Katja Akgün, Tjalf Ziemssen, Björn Falkenburger, Nils Schnalke

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Anika FrankDepartment of Neurology, University Hospital Carl Gustav Carus Dresden, Fetscherstr. 74, 01307, Dresden, Germany.
Jonas ArjomandDepartment of Neurology, University Hospital Carl Gustav Carus Dresden, Fetscherstr. 74, 01307, Dresden, Germany.
Jonas Bendig
Mia DelfsDepartment of Neurology, University Hospital Carl Gustav Carus Dresden, Fetscherstr. 74, 01307, Dresden, Germany.
Lisa KlingelhoeferDepartment of Neurology, University Hospital Carl Gustav Carus Dresden, Fetscherstr. 74, 01307, Dresden, Germany.
Witold H PolanskiDepartment of Neurosurgery, University Hospital Carl Gustav Carus Dresden, Dresden, Germany.
Katja AkgünDepartment of Neurology, University Hospital Carl Gustav Carus Dresden, Fetscherstr. 74, 01307, Dresden, Germany.
Tjalf ZiemssenDepartment of Neurology, University Hospital Carl Gustav Carus Dresden, Fetscherstr. 74, 01307, Dresden, Germany.
Björn FalkenburgerDepartment of Neurology, University Hospital Carl Gustav Carus Dresden, Fetscherstr. 74, 01307, Dresden, Germany. Bjoern.falkenburger@ukdd.de.
Nils SchnalkeDepartment of Neurology, University Hospital Carl Gustav Carus Dresden, Fetscherstr. 74, 01307, Dresden, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Deep brain stimulation (DBS) is an efficient treatment for movement disorders, most commonly Parkinson's Disease (PD), dystonia and essential tremor. DBS surgery carries risks, e.g. the risk of delayed peri-lead edema (PLE) and the risk of postoperative cognitive decline. The mechanisms of these complications are not fully understood and there is no established biomarker to screen for these complications after DBS surgery. To explore the diagnostic value of two blood-based markers representative for distinct types of brain injury, we characterized the dynamics of serum glial fibrillary acidic protein (sGFAP, for glial injury) and serum neurofilament light chain (sNfL, for neuronal-axonal injury) following DBS surgery. We analyzed longitudinal dynamics of serum protein levels in 58 patients undergoing deep brain stimulation (DBS) at our center for half a year post-surgery. Serum GFAP responded much more rapidly after brain surgery, returning to baseline after weeks, whereas sNfL only returned to baseline after months. Patients with lower preoperative cognitive performance exhibited higher postoperative sGFAP levels, with sGFAP showing a stronger association with preoperative patient characteristics compared to sNfL. Further studies with long-term clinical follow-up are needed to fully evaluate the utility of sGFAP as a biomarker for both early and delayed complications after DBS surgery, including cognitive decline and potential foreign body reactions to the implanted lead.

Indexed as

Brain InjuriesCognitive DysfunctionDeep Brain StimulationGlial Fibrillary Acidic ProteinAdultAgedBiomarkersCognitionFemaleHumansMaleMiddle AgedNeurofilament ProteinsParkinson DiseaseBiomarkersGFAP protein, humanGlial Fibrillary Acidic Proteinneurofilament protein LNeurofilament ProteinsDBSDystoniaParkinson’s DiseasesGFAPsNfLTremor

Identifiers

PMID40360583
PMCPMC12075788

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.